The KBG syndrome: An additional sporadic case

Genetic Counseling

Volumn 11, Issue 1, 2000, Pages 33-35

  Mathieu, Michèle ^b   Helou, M ^c   Morin, G ^c   Dolhem, Ph ^c   Devauchelle, B ^a   Piussan, Ch ^c  

^a AMIENS UNIVERSITY HOSPITAL   (France)

^b CHU   (France)

^c NONE

Author keywords

KBG syndrome; Macrodontia; Mental retardation; Skeletal anomalies

Indexed keywords

ARTICLE; CASE REPORT; HUMAN; MALE; MENTAL DEFICIENCY; SKELETON MALFORMATION; TOOTH MALFORMATION;

ABNORMALITIES, MULTIPLE; BONE AND BONES; CHILD; HAND DEFORMITIES, CONGENITAL; HUMANS; MALE; MENTAL RETARDATION; SYNDROME; TOOTH ABNORMALITIES;

EID: 0034050910     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (7)

1. DEVRIENDT K., HOLVOET M., FRYNS J.P.: Further delineation of the KBG syndrome. Genet. Counsel., 1998, 9(3), 191-194.
2. FRYNS J.P., HASPESLAGH M.: Mental retardation, short stature, minor skeletal anomalies, craniofacial dysmorphism and macrodontia in two sisters and their mother. Another variant example of the KBG syndrome? Clin. Genet., 1984, 26, 69-72.
3. HERRMANN, J., PALLISTER P.D., TIDDY W., OPITZ J.M.: The KBG syndrome. A syndrome of short stature, characteristic fades, menial retardation, macrodontia and skeletal abnormalities. Birth defects : original article series, 1975, vol XI, 5, 7-18.
4. PARLOIR C., FRYNS J.P., DEROOVER J., LEBAS E., GOFFAUX P., VAN DEN BERGHE H.: Short stature, craniofacial dysmorphism and dentoskeletal abnormalities in a large kindred. Clin. Genet., 1977, 12, 263-266.
5. SOEKARMAN D., VOLCKE P., FRYNS J.P.: The KBG syndrome: follow-up data on three affected brothers. Clin. Genet., 1994, 46, 283-286.
6. TOLLARO I., BASSARELLI V., CALZOLARI C., PRANCHINI F., COIVANNUCCI UZIELLI ML., VIERI P.L.: Anomalie dentomaxillo-facciali nella «sindrome K.B.G.». Minerva Stomatol., 1984, 33, 437-446.
7. ZOLLINO M., BATTAGLIA A., D'AVANZO M.G., DELLA BRUNA M.M., MARINI R., SCARANO G., CAPPA M., NERI G.: Six additional cases of the KBG syndrome: clinical reports and outline of the diagnostic criteria. Am. J. Med. Genet., 1994, 52, 302-307.